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Oculopharyngeal muscular dystrophy with limb girdle weakness as major complaint
- Source :
- Journal of Neurology, 250, 1307-12, Journal of Neurology, 250, 11, pp. 1307-12
- Publication Year :
- 2003
- Publisher :
- Springer Science and Business Media LLC, 2003.
-
Abstract
- Item does not contain fulltext This first description of the oculopharyngeal muscular dystrophy (OPMD) phenotype in Dutch patients shows that limb girdle weakness can occur early in the course of disease and can give the first and major complaint in OPMD patients. The aim of this study was to examine clinically, histologically and genetically all Dutch OPMD patients known at the Neuromuscular Centre Nijmegen, to measure the limb girdle weakness (MRC scale) and to quantify the consequences of the limb girdle weakness on daily activities (Rankin scale). Remarkable in this population was the early onset and the severity of the limb girdle weakness. We found a higher percentage of patients with limb girdle weakness than reported before in non-Dutch OPMD populations. This limb girdle weakness caused limitations in daily activities more than the other symptoms of OPMD. It was difficult to compare the severity of the limb girdle weakness of Dutch patients with other patients because of the lack of data related to quantification of limb girdle weakness in non-Dutch OPMD patients. Because of the influence of the limb girdle weakness on the daily activities of the patients, we recommend that more attention is paid to the proximal limb muscles in OPMD patients early in the course of the disease.
- Subjects :
- Adult
Male
medicine.medical_specialty
Activities of daily living
Neurology
Biopsy
Population
Poly(A)-Binding Protein II
Polymerase Chain Reaction
Disease course
Oculopharyngeal muscular dystrophy
Muscular Dystrophy, Oculopharyngeal
Blepharoptosis
Humans
Medicine
Muscular dystrophy
Muscle, Skeletal
education
Early onset
education.field_of_study
DNA Repeat Expansion
Muscle Weakness
business.industry
Extremities
Middle Aged
medicine.disease
Neuromuscular development and genetic disorders [UMCN 3.1]
body regions
Limb girdle weakness
Microscopy, Electron
Genetic defects of metabolism [UMCN 5.1]
Physical therapy
Female
Neurology (clinical)
Deglutition Disorders
business
Subjects
Details
- ISSN :
- 14321459 and 03405354
- Volume :
- 250
- Database :
- OpenAIRE
- Journal :
- Journal of Neurology
- Accession number :
- edsair.doi.dedup.....b9a1a0156b9be712e0d1d8edc4d353f4